反应详情

The title compound was prepared according to the procedure in Example 4 using [2-(4-bromo-benzyl)-4,5-dimethyl-furan-3-yl]-(3-cyclopentyl4-hydroxy-phenyl)-methanone (0.203 g, 0.448 mmol) and 4-chlorosulphonyl-2-hydroxybenzoic acid (0.319 g,1.34 mmol). Purification on Dynamax C18 (85% CH3CNIH20) gave 0.221 g (49%) of the title compound as a brown solid, mp 188-192° C. 1H NMR (DMSO-d6) δ1.26-1.32 (m, 2 H), 1.49-1.57 (m, 2 H), 1.64-1.74 (m, 4 H), 1.77 (s, 3 H), 2.18 (s, 3 H), 2.96 (quintet, 1 H), 3,79 (s, 2 H), 6.96 (d, 2 H), 7.23 (d, 1 H), 7.36 -7.43 (m, 4 H), 7.53-7.56 (m, 2 H), 8.00 (d, 1 H). IR (KBr) 3400, 2950, 1690, 1390 and 1190 cm−1. mass spectrum (−ESI) m/z 651 (M−H). Anal. Calcd. for C32H29BrO8S: C, 58.81; H, 4.47; N, 0.00. Found: C, 58.45; H. 4.54; N, 0.07.

1. customThe title compound was prepared
2. customPurification on Dynamax C18 (85% CH3CNIH20)